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Results: 1-14 |
Results: 14
Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions
Authors: Van Goethem, G Dermaut, B Lofgren, A Martin, JJ Van Broeckhoven, C
Citation: G. Van Goethem et al., Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions, NAT GENET, 28(3), 2001, pp. 211-212
The TNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease
Authors: Theuns, J Feuk, L Dermaut, B Del-Favero, J Roks, G Van den Bossche, D Corsmit, E Van den Broeck, M van Duijn, CM Cruts, M Brookes, AJ Van Broeckhoven, C
Citation: J. Theuns et al., The TNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease, HUM GENET, 108(6), 2001, pp. 552-553
Variable expression of presenilin 1 is not a major determinant of risk forlate-onset Alzheimer's Disease
Authors: Dermaut, B Roks, G Theuns, J Rademakers, R Houwing-Duistermaat, JJ Serneels, S Hofman, A Breteler, MMB Cruts, M Van Broeckhoven, C van Duijn, CM
Citation: B. Dermaut et al., Variable expression of presenilin 1 is not a major determinant of risk forlate-onset Alzheimer's Disease, J NEUROL, 248(11), 2001, pp. 935-939
Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt-Jakob Disease phenotype
Authors: Van Everbroeck, B Croes, EA Pals, P Dermaut, B Jansen, G van Duijn, CM Cruts, M Van Broeckhoven, C Martin, JJ Cras, P
Citation: B. Van Everbroeck et al., Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt-Jakob Disease phenotype, NEUROSCI L, 313(1-2), 2001, pp. 69-72
Amyloid beta secretase gene (BACE) is neither mutated in nor associated with early-onset Alzheimer's disease
Authors: Cruts, M Dermaut, B Rademakers, R Roks, G Van den Broeck, M Munteanu, G van Duijn, CM Van Broeckhoven, CV
Citation: M. Cruts et al., Amyloid beta secretase gene (BACE) is neither mutated in nor associated with early-onset Alzheimer's disease, NEUROSCI L, 313(1-2), 2001, pp. 105-107
The cystatin C polymorphism is not associated with early onset Alzheimer'sdisease
Authors: Roks, G Cruts, M Slooter, AJC Dermaut, B Hofman, A Van Broeckhoven, C Van Duijn, CM
Citation: G. Roks et al., The cystatin C polymorphism is not associated with early onset Alzheimer'sdisease, NEUROLOGY, 57(2), 2001, pp. 366-367
CAG repeat expansion in the TATA box-binding protein gene causes autosomaldominant cerebellar ataxia
Authors: Fujigasaki, H Martin, JJ De Deyn, PP Camuzat, A Deffond, D Stevanin, G Dermaut, B Van Broeckhoven, C Durr, A Brice, A
Citation: H. Fujigasaki et al., CAG repeat expansion in the TATA box-binding protein gene causes autosomaldominant cerebellar ataxia, BRAIN, 124, 2001, pp. 1939-1947
Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression
Authors: Theuns, J Del-Favero, J Dermaut, B van Duijn, CM Backhovens, H Van den Broeck, M Serneels, S Corsmit, E Van Broeckhoven, C Cruts, M
Citation: J. Theuns et al., Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression, HUM MOL GEN, 9(3), 2000, pp. 325-331
Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin1 missense substitution and a prion protein gene insertion
Authors: Dermaut, B Cruts, M Backhovens, H Lubke, U Van Everbroeck, B Sciot, R Dom, R Martin, JJ Van Broeckhoven, C Cras, P
Citation: B. Dermaut et al., Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin1 missense substitution and a prion protein gene insertion, J NEUROL, 247(5), 2000, pp. 364-368
The alpha 2-macroglobulin gene in AD - A population-based study and meta-analysis
Authors: Koster, MN Dermaut, B Cruts, M Houwing-Duistermaat, JJ Roks, G Tol, J Ott, A Hofman, A Munteanu, G Breteler, MMB van Duijn, CM Van Broeckhoven, C
Citation: Mn. Koster et al., The alpha 2-macroglobulin gene in AD - A population-based study and meta-analysis, NEUROLOGY, 55(5), 2000, pp. 678-684
Genetic testing should not be advocated as a diagnostic tool in familial forms of dementia
Authors: Croes, EA Dermaut, B van der Cammen, TJM van Broeckhoven, C van Duijn, CM
Citation: Ea. Croes et al., Genetic testing should not be advocated as a diagnostic tool in familial forms of dementia, AM J HU GEN, 67(4), 2000, pp. 1033-1035
Mutation screening of the tau gene in patients with early-onset Alzheimer's disease
Authors: Roks, G Dermaut, B Heutink, P Julliams, A Backhovens, H Van de Broeck, M Serneels, S Hofman, A Van Broeckhoven, C van Duijn, CM Cruts, M
Citation: G. Roks et al., Mutation screening of the tau gene in patients with early-onset Alzheimer's disease, NEUROSCI L, 277(2), 1999, pp. 137-139
The Glu318Gly substitution in presenilin 1 is not causally related to Alzheimer disease
Authors: Dermaut, B Cruts, M Slooter, AJC Van Gestel, S De Jonghe, C Vanderstichele, H Vanmechelen, E Breteler, MM Hofman, A van Duijn, CM Van Broeckhoven, C
Citation: B. Dermaut et al., The Glu318Gly substitution in presenilin 1 is not causally related to Alzheimer disease, AM J HU GEN, 64(1), 1999, pp. 290-292
Glu318Gly in presenilin-1 is a neutral mutation in relation to dementia: The Rotterdam study
Authors: Dermaut, B Cruts, M Slooter, AJC Van Gestel, S De Jonghe, C Backhovens, H Vanderstichele, H Vanmechelen, E Breteler, MMB Hofman, A Hendriks, L Van Duijn, CM Van Broeckhoven, C
Citation: B. Dermaut et al., Glu318Gly in presenilin-1 is a neutral mutation in relation to dementia: The Rotterdam study, ALZHEIMER'S DISEASE AND RELATED DISORDERS, 1999, pp. 87-92
Risultati: 1-14 |